Cardio-Oncology Program and CardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Curr Oncol Rep. 2018 Apr 11;20(6):44. doi: 10.1007/s11912-018-0690-1.
This review describes cardiotoxicity associated with adoptive T cell therapy and immune checkpoint blockade.
Cardiotoxicity is a rare but potentially fatal complication associated with novel immunotherapies. Both affinity-enhanced and chimeric antigen receptor T cells have been reported to cause hypotension, arrhythmia, and left ventricular dysfunction, typically in the setting of cytokine release syndrome. Immune checkpoint inhibitors are generally well-tolerated but have the potential to cause myocarditis, with clinical presentations ranging from asymptomatic cardiac biomarker elevation to heart failure, arrhythmia, and cardiogenic shock. Electrocardiography, cardiac biomarker measurement, and cardiac imaging are key components of the diagnostic evaluation. For suspected myocarditis, endomyocardial biopsy is recommended if the diagnosis remains unclear after initial testing. The incidence of immunotherapy-associated cardiotoxicity is likely underestimated and may increase as adoptive T cell therapy and immune checkpoint inhibitors are used in larger populations and for longer durations of therapy. Baseline and serial cardiac evaluation is recommended to facilitate early identification and treatment of cardiotoxicity.
本文描述了过继性 T 细胞治疗和免疫检查点阻断相关的心脏毒性。
心脏毒性是新型免疫疗法罕见但潜在致命的并发症。亲和力增强型和嵌合抗原受体 T 细胞均已被报道导致低血压、心律失常和左心室功能障碍,通常发生在细胞因子释放综合征的背景下。免疫检查点抑制剂通常具有良好的耐受性,但有可能引起心肌炎,临床表现从无症状性心脏生物标志物升高到心力衰竭、心律失常和心源性休克不等。心电图、心脏生物标志物测量和心脏成像是诊断评估的关键组成部分。对于疑似心肌炎,如果初始检查后诊断仍不明确,则建议进行心内膜心肌活检。随着过继性 T 细胞治疗和免疫检查点抑制剂在更大人群中使用更长时间,免疫治疗相关心脏毒性的发生率可能被低估,并可能增加。建议进行基线和连续的心脏评估,以促进心脏毒性的早期识别和治疗。